Mirati Therapeutics to Report Third Quarter 2022 Financial Results and Recent Corporate Updates

On October 25, 2022 Mirati Therapeutics, Inc. (NASDAQ: MRTX), a clinical-stage targeted oncology company, reported that it will announce financial results for the third quarter of 2022 along with recent corporate updates on November 8, 2022 (Press release, Mirati, OCT 25, 2022, https://www.prnewswire.com/news-releases/mirati-therapeutics-to-report-third-quarter-2022-financial-results-and-recent-corporate-updates-301659038.html [SID1234622370]). During a conference call at 4:30 p.m. ET / 1:30 p.m. PT on November 8, company executives will provide company updates and review financial results.

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Investors and the general public are invited to listen to a live webcast of the call at the "Investors and Media" section on Mirati.com or by dialing the U.S. toll free +1 773-305-6853 or international +1 866-409-1555, confirmation code: 8269398. A replay of the call will be available approximately 2 hours after the event has ended at the same website.

Perrigo to Release Third Quarter 2022 Financial Results on November 8, 2022

On October 25, 2022 Perrigo Company plc (NYSE: PRGO), a leading provider of Consumer Self-Care Products, reported that it will release its third quarter 2022 financial results on Tuesday, November 8, 2022 (Press release, Perrigo Company, OCT 25, 2022, View Source [SID1234622369]). The Company will also host a conference call beginning at 8:30 A.M. (EST).

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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The conference call will be available live via webcast to interested parties in the investor relations section of the Perrigo website at View Source or by phone at 888-317-6003, International 412-317-6061, and reference ID # 8518983. A taped replay of the call will be available beginning at approximately 12:00 P.M. (EST) Tuesday, November 8, until midnight Tuesday, November 15, 2022. To listen to the replay, dial 877-344-7529, International 412-317-0088, and use access code 7261267.

Nektar to Announce Financial Results for the Third Quarter 2022 on Thursday, November 3, 2022, After Close of U.S.-Based Financial Markets

On October 25, 2022 Nektar Therapeutics (Nasdaq: NKTR) reported that it will announce its financial results for the third quarter 2022 on Thursday, November 3, 2022, after the close of U.S.-based financial markets (Press release, Nektar Therapeutics, OCT 25, 2022, View Source [SID1234622368]). Howard Robin, President and Chief Executive Officer, will host a conference call to review the results beginning at 5:00 p.m. Eastern Time/2:00 p.m. Pacific Time.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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The press release and live audio-only webcast of the conference call can be accessed through a link that is posted on the Home Page and Investors section of the Nektar website: View Source The web broadcast of the conference call will be available for replay through December 3, 2022.

To access the conference call, please pre-register at Nektar Earnings Call Registration. All registrants will receive dial-in information and a PIN allowing them to access the live call.

Koneksa Announces Clinical Pipeline of Validated Digital Biomarkers to Accelerate Life Sciences Research

On October 25, 2022 Koneksa, a healthcare technology company developing evidence-based validated digital biomarkers, reported the launch of its clinical pipeline featuring biomarkers across neuroscience, oncology, respiratory, and other therapeutic areas (Press release, Koneksa, OCT 25, 2022, View Source [SID1234622367]). With 15 digital biomarker programs in development, the company will also be launching several upcoming clinical studies. Koneksa and collaborators have published more than 20 peer-reviewed papers.

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Koneksa’s digital biomarker platform uses algorithms to analyze and integrate real-time patient data into clinical trials, translating typically analog processes into digital. By developing a suite of validated, evidence-based digital biomarker solutions that can be seamlessly integrated into clinical studies, from at-home spirometry, actigraphy, gait and balance-monitoring tools, to vital-sign monitoring, Koneksa’s biomarker technology potentially increases precision and captures a richer dataset.

The launch of the clinical pipeline will enable Koneksa to expand biomarker evidence generation in the near-term and develop new digital biomarkers to support long-term industry and patient needs. The increasing adoption of clinically-validated digital biomarkers in studies which can be used in an at-home setting, significantly reduces patient burden and increases clinical trial efficiency. Digital biomarkers can also integrate data from multiple sources to help researchers better understand key drivers of disease progression to bring novel medicines to patients faster.

"Digital biomarkers need to be clinically validated. Without that validation, these tools are ultimately not useful in clinical trials," said Chris Benko, CEO & Founder of Koneksa. "Think of digital biomarkers versus a clinic-based assessment as the difference between a still photo and a video. A still photo is great, but a video can tell a much richer story. Over the last few years, our team has conducted over a dozen analytical studies, with the same level of clinical rigor to validate our digital biomarkers on par with traditional biomarkers for use in clinical trials."

"The more high quality measurements we capture, the higher precision and more power a clinical trial can have," said John Wagner, M.D., Ph.D., Chief Medical Officer, Koneksa. "Validation studies have shown that our digital biomarkers are equivalent to or better than the current standard – and we have done that work to the level of rigor required by regulators and the world’s leading biopharmaceutical companies. With the launch of our clinical pipeline, we’re extending our evidence generation and potential new digital biomarkers, further demonstrating that at-home digital biomarkers increase patient access outside of the clinic."

Koneksa has partnerships with life sciences companies, patient advocacy organizations and academic institutions on its digital biomarker pipeline. In respiratory disease, Koneksa partnered with Regeneron to implement and validate mobile spirometry. In oncology, Koneksa developed a step count measurement, in partnership with Montefiore Medical Center, to better characterize functional status. In neuroscience, the company partnered with Sanofi to develop biomarkers to measure gait in patients with neurological diseases such as multiple sclerosis. Koneksa recently announced a partnership with Aural Analytics to support clinical trials using speech measures to develop a variety of digital biomarkers for Parkinson’s Disease in collaboration with Northwestern University and the Michael J. Fox Foundation.

Koneksa’s development and validation process for its digital biomarker solutions is based on the same FDA guidelines and level of rigor for traditional biomarkers such as the Biomarker Qualification Evidentiary Framework as well as the Digital Health Technologies Remote Data Acquisition In Clinical Investigations draft guidance.

Koneksa will also be hosting the grand opening of its new global headquarters on the 77th floor of One World Trade Center in New York City on Thursday, November 10th, 5:30-8:00 pm ET. Interested media can RSVP to [email protected] to tour our facility, learn more about our operations, and come meet the Koneksa team and our supporters.

Similis Bio Partners With Blau Farmaceutica to Co-Develop Four Biosimilar Programs

On October 25, 2022 JSR Life Sciences, LLC (JSR) and Blau Farmaceutica (Blau) (public company in Brazil B3 – BLAU3) reported that Similis Bio ("Similis"), its recently launched business unit focused on biosimilar development, has signed its first development and license agreement with Blau Farmacêutica ("Blau") (Press release, JLS, OCT 25, 2022, View Source [SID1234622366]). The agreement, Blau’s most recent move into the biosimilars market, is a multi-product and multi-year deal to develop products and licenses IP for four biosimilar assets targeting indications in oncology, inflammation, and blood disorders.

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"We launched Similis Bio as we saw the need to mitigate risk and accelerate timelines for biosimilar developers," said John Gabrielson, Senior Vice President at JSR Life Sciences and Head of Similis Bio. "We are thrilled to partner with Blau as they work to launch their biosimilar business initially in North and South America. We look forward to leveraging our expertise and experience to support programs that can provide additional treatment options for some of the most debilitating diseases patients face."

Similis Bio will provide full processes and associated IP for tech transfer to Blau, including cell lines, analytical data and methodologies, and upstream/downstream processes. Blau will utilize the licensed IP for GMP manufacturing and clinical development and seek regulatory approval.

Blau has exclusive worldwide rights and intent to sell in America by itself and partner with local organizations in other regions. The agreement is structured with upfront payments and long-term royalties upon commercial approval for sale. Blau and Similis expect the total value of the contract to exceed USD 100 million. The Companies are not disclosing additional financial terms.

These four biosimilars have an addressable market in the world of more than USD 42 billion and, in Brazil, of close to USD 1 billion, according to IQVIA, ensuring a robust pipeline for the Company in the long term.

The launch of these drugs will be a milestone in the history of Blau and Brazil, which will have a local producer developing and producing APIs (Active Pharmaceutical Ingredients) and biosimilar medicines in line with the national policy of independence in the production of APIs.

"This initiative will give the world population greater access to advanced medicines, raising the standard of care. Blau continues to invest at a strong pace in the development of new APIs and new highly complex drugs, in addition to expanding its production capacity, geographic presence, and relevance in the health industry," said Roberto Morais, Executive Director in Charge of M&A and Strategic Alliances. "We are developing products for the next decade, and we will further add new products to our partnership. This strategic and disruptive agreement reinforces Blau’s position in becoming a reference in the production of biosimilars in Latin America."